A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421709



Internal ID21079262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42165428..42168716hg38UCSC Ensembl
chr8:42022946..42026234hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg383289
hg193289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166945
Samples
Known GenesAP3M2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421709
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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